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Endocrinology, ISSN 0013-7227, 08/2010, Volume 151, Issue 8, pp. 3514 - 3520
Prostate cancer usually responds to androgen deprivation therapy, although the response in metastatic disease is almost always transient and tumors eventually... 
Journal Article
Journal Article
Cancer Research, ISSN 0008-5472, 08/2015, Volume 75, Issue 15 Supplement, pp. 225 - 225
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 08/2011, Volume 108, Issue 33, p. 13728
In the majority of cases, advanced prostate cancer responds initially to androgen deprivation therapy by depletion of gonadal testosterone. The response is... 
Testosterone | Castration | Rodents | Biosynthesis | Gene expression | Prostate cancer
Journal Article
Endocrinology, ISSN 0013-7227, 09/2009, Volume 150, Issue 9, pp. 4154 - 4162
Human 17β-hydroxysteroid dehydrogenase types 1 and 2 (17βHSD1 and 17βHSD2) regulate estrogen potency by catalyzing the interconversion of estrone (E1) and... 
3-DIMENSIONAL STRUCTURE | HYDROXYSTEROID DEHYDROGENASES | SUBSTRATE-BINDING | REDOX STATE | LIVER | ENDOCRINOLOGY & METABOLISM | SCOR ENZYME FAMILY | 20-ALPHA-HYDROXYSTEROID DEHYDROGENASE | ENDOPLASMIC-RETICULUM | COFACTOR | ALDO-KETO REDUCTASE
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 10/2006, Volume 91, Issue 10, pp. 4179 - 4182
Context: Congenital adrenal hyperplasia resulting from 17α-hydroxylase deficiency (17OHD) is a rare disorder associated with hypertension. Subject and Methods:... 
CYP17 GENE | ENDOCRINOLOGY & METABOLISM | BRAZILIAN PATIENTS | MALE PSEUDOHERMAPHRODITISM | P450C17 | 17-HYDROXYLASE DEFICIENCY | JAPANESE PATIENTS | IDENTIFICATION | MOLECULAR-BASIS | BIOCHEMICAL-DIAGNOSIS | 17,20-LYASE DEFICIENCY
Journal Article
The Journal of clinical endocrinology and metabolism, ISSN 0021-972X, 10/2006, Volume 91, Issue 10, p. 4179
Congenital adrenal hyperplasia resulting from 17alpha-hydroxylase deficiency (17OHD) is a rare disorder associated with hypertension. We describe a... 
Humans | Adult | Female | Male | Steroid 17-alpha-Hydroxylase - genetics | Adrenal Hyperplasia, Congenital - genetics | Mutation
Journal Article
Arquivos Brasileiros de Endocrinologia e Metabologia, ISSN 0004-2730, 11/2010, Volume 54, Issue 8, pp. 744 - 748
Journal Article
Journal Article
Arquivos Brasileiros de Endocrinologia & Metabologia, ISSN 1677-9487, 11/2010, Volume 54, Issue 8, pp. 744 - 748
Congenital adrenal hyperplasia (CAH) resulting from 17α-hydroxylase/17,20-lyase deficiency is a rare autosomal recessive disease and the second most common... 
ENDOCRINOLOGY & METABOLISM
Journal Article
ARQUIVOS BRASILEIROS DE ENDOCRINOLOGIA E METABOLOGIA, ISSN 0004-2730, 11/2010, Volume 54, Issue 8, pp. 744 - 748
m Congenital adrenal hyperplasia (CAH) resulting from 17 alpha-hydroxylase/17,20-lyase deficiency is a rare autosomal recessive disease and the second most... 
P450C17 DEFICIENCY | CLONING | LYASE | ENDOCRINOLOGY & METABOLISM | 17,20-LYASE DEFICIENCY | Hypogonadism - genetics | Homozygote | Humans | Adolescent | Brazil | Female | Steroid 17-alpha-Hydroxylase - genetics | Adrenal Hyperplasia, Congenital - genetics | Hypertension - genetics | Mutation - genetics
Journal Article
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